Screening of the TMEM151A Gene in Patients With Paroxysmal Kinesigenic Dyskinesia and Other Movement Disorders

BACKGROUND: Paroxysmal kinesigenic dyskinesia (PKD) is a rare neurological disorder characterized by recurrent involuntary movements usually triggered by sudden movements. Mutations in the TMEM151A gene were found to be the causative factor of PKD in recent studies. It has also been revealed that lo...

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Detalles Bibliográficos
Autores principales: Ma, Ling-Yan, Han, Lin, Niu, Meng, Chen, Lu, Yu, Ya-Zhen, Feng, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189402/
https://www.ncbi.nlm.nih.gov/pubmed/35707035
http://dx.doi.org/10.3389/fneur.2022.865690

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189402/
https://www.ncbi.nlm.nih.gov/pubmed/35707035
http://dx.doi.org/10.3389/fneur.2022.865690

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